首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >The perioperative patient on buprenorphine: a systematic review of perioperative management strategies and patient outcomes
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The perioperative patient on buprenorphine: a systematic review of perioperative management strategies and patient outcomes

机译:对丁丙诺啡的围手术期患者:围手术期管理策略和患者结果的系统审查

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BackgroundAn increasing number of patients with opioid use disorder (OUD) are treated with opioid agonist-antagonists such as buprenorphine/naloxone. Perioperative management of patients on buprenorphine/naloxone is inconsistent and remains a controversial topic with mismanagement posing a significant risk to the long-term health of these patients.MethodsWe performed a systematic literature search involving Medline, Medline In-Process, Embase, Cochrane Central, Cochrane Database of Systematic Reviews, PsycINFO, Web of Science (Clarivate), Scopus (Elsevier), CINAHL (EbscoHosst), and PubMed (NLM).ResultsEighteen studies were included in the final sample, including one controlled study and four observational studies . Neither the controlled study nor the observational studies assessed addiction treatment retention, harm reduction, or long-term mortality rates as primary or secondary outcomes. Of the observational studies, authors showed equivalent peri- and postoperative pain control among buprenorphine continued patients. All but one authors described adequate analgesia among the case reports in which buprenorphine 16 mg sublingually (SL) daily was continued during the perioperative period. Long-term harm reduction was not reported with only three case reports including any long-term abstinence or relapse rates.ConclusionsThe current understanding of the risks and benefits of continuing or stopping buprenorphine perioperatively is limited by a lack of high-quality evidence. Observational studies and case reports indicate no evidence against continuing buprenorphine perioperatively, especially when the dose is 16 mg SL daily. In patients with significant potential for relapse, such as those with a recent history of OUD, the discontinuation of buprenorphine should have a strong rationale supported by patient and surgical preferences. Future studies require standardized reporting of median doses, details on the route of delivery, dosing schedules and any dosing changes, and rates of addiction relapse, including long-term morbidity and mortality where possible.
机译:背景越来越多的阿片类药物使用障碍(OUD)患者接受阿片类激动剂拮抗剂治疗,如丁丙诺啡/纳洛酮。丁丙诺啡/纳洛酮患者的围手术期管理不一致,仍然是一个有争议的话题,管理不善对这些患者的长期健康构成重大风险。方法我们进行了系统的文献检索,涉及Medline、Medline In Process、Embase、Cochrane Central、Cochrane系统评价数据库、PsycINFO、科学网(Clarivate)、Scopus(Elsevier)、CINAHL(EbscoHosst)和PubMed(NLM)。结果最终样本包括八项研究,包括一项对照研究和四项观察性研究。无论是对照研究还是观察性研究,都没有将成瘾治疗保留、减少伤害或长期死亡率作为主要或次要结果进行评估。在观察性研究中,作者显示丁丙诺啡持续治疗的患者的围手术期和术后疼痛控制相当。除一名作者外,所有作者均在病例报告中描述了充分的镇痛作用,其中在围手术期持续使用丁丙诺啡(SL)每日16 mg舌下给药。只有三例病例报告(包括任何长期禁欲或复发率)未报告长期伤害减少。结论由于缺乏高质量的证据,目前对继续或停止丁丙诺啡围手术期治疗的风险和益处的理解受到限制。观察性研究和病例报告表明,没有证据表明丁丙诺啡可以在围手术期继续使用,尤其是当剂量为;每天16毫克SL。对于有明显复发可能性的患者,如近期有OUD病史的患者,停用丁丙诺啡应有一个强有力的理由,并得到患者和手术偏好的支持。未来的研究需要标准化地报告中位剂量、给药途径、给药时间表和任何给药变化的细节,以及成瘾复发率,包括长期发病率和死亡率(如可能)。

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